SEBIA CAPICLEAN CAPILLARYS 3 - Indonesia BPOM Medical Device Registration
SEBIA CAPICLEAN CAPILLARYS 3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204320501. The device is manufactured by SEBIA from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PROSPEROUS ADVANCED ERA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
SEBIACountry of Origin
France
Authorized Representative
PT. PROSPEROUS ADVANCED ERAAR Address
Ruko Puri Botanical Junction Blok H7 / 17 Rt.007/01 Jl.Raya Joglo Kembangan - Jakarta Barat
Registration Date
Jun 24, 2023
Expiry Date
Aug 31, 2025
Product Type
Reagents and Specimen Providers
General purpose reagent.
Invitro Diagnostics
FLUIDIL
SEBIA Antisera K & L Free Light Chains
CSF Control
MINICAP HbA1c
SEBIA Hydrasys 2 Scan Focusing
HYDRAGEL 3 CSF ISOFOCUSING
HYDRASYS Wash Solution
SEBIA Destaining Solution
MINICAP HEMOGLBIN (E)
SEBIA CAPILLARY 3 OCTA
STAGO sthemO PT M
DIAGNOSTICA STAGO S.A.S
STAGO sthemO VWF Cal
DIAGNOSTICA STAGO S.A.S
STHEMO Thrombin M
DIAGNOSTICA STAGO S.A.S
STAGO sthemO Unical
DIAGNOSTICA STAGO S.A.S
SD lnnovation TA-4V Aggregometer
SD INNOVATION S.A.S
STAGO sthemO CaCl2 M
DIAGNOSTICA STAGO S.A.S
STHEMO PTT A
DIAGNOSTICA STAGO S.A.S
sthemO Fib M
DIAGNOSTICA STAGO S.A.S
Stago Themo Oren Kaler M
DIAGNOSTICA STAGO S.A.S
FLUIDIL
SEBIA